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Andrew R Jackson

Showing results (1-10 of 15) with videos related to

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Genome Research|April 3, 2004
Pash: efficient genome-scale sequence anchoring by Positional HashingKen J Kalafus, Andrew R Jackson, Aleksandar Milosavljevic
BMC Bioinformatics|January 14, 2012
An integrative variant analysis suite for whole exome next-generation sequencing dataDanny Challis, Jin Yu, Uday S Evani, et al.
Nature Communications|February 19, 2015
Epigenomic footprints across 111 reference epigenomes reveal tissue-specific epigenetic regulation of lincRNAsViren Amin, R Alan Harris, Vitor Onuchic, et al.
BMC Genomics|November 9, 2012
Atlas2 Cloud: a framework for personal genome analysis in the cloudUday S Evani, Danny Challis, Jin Yu, et al.
Genome Research|September 11, 2012
Spark: a navigational paradigm for genomic data explorationCydney B Nielsen, Hamid Younesy, Henriette O'Geen, et al.
Genome Research|February 3, 2005
Pooled genomic indexing of rhesus macaqueAleksandar Milosavljevic, Ronald A Harris, Erica J Sodergren, et al.
Human Mutation|October 13, 2018
ClinGen Allele Registry links information about genetic variantsPiotr Pawliczek, Ronak Y Patel, Lillian R Ashmore, et al.
Genome Medicine|January 14, 2017
ClinGen Pathogenicity Calculator: a configurable system for assessing pathogenicity of genetic variantsRonak Y Patel, Neethu Shah, Andrew R Jackson, et al.
Bioinformatics (Oxford, England)|January 20, 2026
Aggregation of gene regulatory information and knowledge on FAIR principles enables discovery of pathogenic gene regulatory variantsKeyang Yu, Haoquan Zhao, Andrea Wilderman, et al.
Cell Genomics|April 9, 2026
ClinGen API platform for classification of human genetic variantsNeethu Shah, Tierra Farris, Arturo Alejandro Zuniga, et al.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
Genome Research|April 3, 2004
Pash: efficient genome-scale sequence anchoring by Positional HashingKen J Kalafus, Andrew R Jackson, Aleksandar Milosavljevic
BMC Bioinformatics|January 14, 2012
An integrative variant analysis suite for whole exome next-generation sequencing dataDanny Challis, Jin Yu, Uday S Evani, et al.
Nature Communications|February 19, 2015
Epigenomic footprints across 111 reference epigenomes reveal tissue-specific epigenetic regulation of lincRNAsViren Amin, R Alan Harris, Vitor Onuchic, et al.
BMC Genomics|November 9, 2012
Atlas2 Cloud: a framework for personal genome analysis in the cloudUday S Evani, Danny Challis, Jin Yu, et al.
Genome Research|September 11, 2012
Spark: a navigational paradigm for genomic data explorationCydney B Nielsen, Hamid Younesy, Henriette O'Geen, et al.
Genome Research|February 3, 2005
Pooled genomic indexing of rhesus macaqueAleksandar Milosavljevic, Ronald A Harris, Erica J Sodergren, et al.
Human Mutation|October 13, 2018
ClinGen Allele Registry links information about genetic variantsPiotr Pawliczek, Ronak Y Patel, Lillian R Ashmore, et al.
Genome Medicine|January 14, 2017
ClinGen Pathogenicity Calculator: a configurable system for assessing pathogenicity of genetic variantsRonak Y Patel, Neethu Shah, Andrew R Jackson, et al.
Bioinformatics (Oxford, England)|January 20, 2026
Aggregation of gene regulatory information and knowledge on FAIR principles enables discovery of pathogenic gene regulatory variantsKeyang Yu, Haoquan Zhao, Andrea Wilderman, et al.
Cell Genomics|April 9, 2026
ClinGen API platform for classification of human genetic variantsNeethu Shah, Tierra Farris, Arturo Alejandro Zuniga, et al.
Pageof 2